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  • ¿µ¹®
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  • Kallmann syndrome
    Ä®¸¸ÁõÈıº
  • Kartagener¡¯s syndrome
    Ä«¸£Å¸°Ô³ÊÁõÈıº
  • Klinefelter¡¯s syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº
  • Klippel-Feil syndrome
    Ŭ¸®Æç-ÆÄÀÏÁõÈıº
  • Korsakoff¡¯s syndrome
    ÄÚ¸£»çÄÚÇÁÁõÈıº
  • Kearns-Sayre syndrome
    ÄÁ½º-¼¼À̾îÁõÈıº
  • late dumping syndrome
    ¸¸±â´ýÇÎÁõÈıº
  • Laurence-Moon syndrome
    ·Î·»½º-¹®ÁõÈıº
  • Lennox-Gastaut syndrome
    ·¹³ì½º-°¡½ºÅäÁõÈıº
  • Lesch-Nyhan syndrome
    ·¹½´-´ÏÇÑÁõÈıº
  • Libman-Sacks syndrome
    ¸®ºê¸Õ-»è½ºÁõÈıº
  • locked-in syndrome
    °¨±ÝÁõÈıº
  • long QT syndrome
    ±äQTÁõÈıº
  • lymphadenopathy syndrome
    ¸²ÇÁÀýº´(Áõ)ÁõÈıº
  • lymphoproliferative syndrome
    ¸²ÇÁ¼¼Æ÷Áõ½ÄÁõÈıº
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  • maladaptation syndrome
    ÀûÀÀÀå¾ÖÁõÈıº
  • maltreatment syndrome
    ÇдëÁõÈıº
  • maternal deprivation syndrome
    ¸ð¼º¹ÚÅ»ÁõÈıº
  • megacystis-megaureter syndrome
    Å«¹æ±¤Å«¿ä°üÁõÈıº
  • meningeal irritation syndrome
    ¼ö¸·ÀÚ±ØÁõÈıº
  • midsystolic click syndrome
    ¼öÃàÁß±âŬ¸¯ÁõÈıº
  • morning glory syndrome
    ³ªÆÈ²ÉÁõÈıº
  • motor syndrome
    ¿îµ¿ÁßÃßÁõÈıº
  • myasthenic syndrome
    ±ÙÀ°¹«·ÂÁõÈıº
  • myelodysplastic syndrome
    °ñ¼öÇü¼ºÀÌ»óÁõÈıº
  • myeloproliferative syndrome
    °ñ¼öÁõ½ÄÁõÈıº
  • myofascial click pain syndrome
    ±Ù¸·ÅëÁõÁõÈıº
  • myotonic syndrome
    ±ÙÀ°±äÀåÁõÈıº
  • naviculocapitate syndrome
    ¼Õ¹è¾Ë¸Ó¸®»ÀÁõÈıº
  • nephrotic syndrome
    ÄáÆÏÁõÈıº
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  • Lambert-Eaton myasthenic syndrome
    ¶÷¹öÆ®-ÀÌÆ° ±Ù¹«·ÂÁõÁõÈıº
  • Landry Guillain Barre syndrome
    ¶õµå¸®-±æ·©-¹Ù·¹ÁõÈıº.
  • Laurence Moon Biedl syndrome
    ·Î·»½º-¹®-ºñµéÁõÈıº.
  • Lesch-Nyhan syndrome
    ·¹½¬ ´ÏÇÑ ÁõÈıº
  • Leser-Trelat syndrome
    ·¹Á¦¸£ Æ®·¼¶ó ÁõÈıº
  • Lhermittes syndrome, radiation-induced
    ¹æ»ç¼±À¸·Î À¯¹ßµÈ ·¹¹ÌÅ× ÁõÈıº
  • Libman Sachs syndrome
    ¸®ºê¸¸-ÀÛ½º ÁõÈıº.
  • Loeffler s eosinophilic syndrome
    ·ÚÇ÷¯È£»ê±¸ÁõÈıº
  • Loeffler s eosinophilic syndrome
    ·ÚÇ÷¯È£»ê±¸ÁõÈıº.
  • Loefflers syndrome
    ·ÚÇ÷¯ÁõÈıº
  • Lofgrens syndrome
    ·ÚÇÁ ±×¸° ÁõÈıº
  • Marchesanis syndrome
    ¸¶¸£ÄÉ»ç´ÏÁõÈıº
  • Marcus-Gunn syndrome
    ¸¶¸£Äí½º-°ÇÁõÈıº
  • Marfan s syndrome
    ¸¶¸£ÆÎÁõÈıº
  • Marfan s syndrome
    ¸¶¸£ÆÎÁõÈıº.
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  • spinal mydriasis
    ô¼ö¼º »êµ¿(ô±âÐàõߤÔÚ).
  • spinal mydriasis
    ô¼ö¼º »êµ¿(ô±âÐàõߤÔÚ)
  • spinal myotome
    ôÃß±ÙÀ°ºÐÀý
  • spinal nerve trunk
    ô¼ö½Å°æÁÙ±â
  • spinal nerves
    ô¼ö½Å°æ(¡­ãêÌè).
  • spinal nerves
    ô¼ö½Å°æ
  • spinal nucleus of trigeminal nerve
    »ïÂ÷½Å°æÃ´¼öÇÙ
  • spinal nystagmus
    ô¼ö¼º ¾ÈÁø(¡­äÑòè)
  • spinal nystagmus
    ô¼ö¼º ¾ÈÁø(¡­äÑòè).
  • spinal pachymeningitis
    ô¼ö°æ¸·¿° (¡­ دæú).
  • spinal pachymeningitis
    ô¼ö°æ¸·¿° (¡­ÌãØ¯æú)
  • spinal paralysis
    ô¼ö¸¶ºñ(¡­ Ýö).
  • spinal paralysis
    ô¼ö¸¶ºñ(¡­Ø«Ýö)
  • spinal paralytic polio
    ô¼öÇü ¸¶ºñ¼º Æú¸®¿À(ô±âÐû¡Ø«Ýöàõ¡­ )
  • spinal parasympathetic
    ô¼öºÎ±³°¨½Å°æ (¡­ÜùÎßÊïãêÌè).
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SCC self-care center; sequential combination chemotherapy; services for crippled children; short-course ...
SCEP sandwich counterelectrophoresis; spinal cord evoked potential
SCI Science Citation Index; spinal cord injury; structured clinical interview
SCIM spinal cord injury medicine
SCIS spinal cord injury service
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 14
ARN Acute retinal necrosis syndrome
ATLS Acute tumor lysis syndrome
AGS Adrenogenital Syndrome
AGS Alagille syndrome
AWS Alcohol Withdrawal Syndrome
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  • dyskinetic syndrome
    ¿îµ¿ Àå¾Ö ÁõÈıº
  • dysplastic nevus syndrome
    ÀÌÇü¼º ¸ð¹Ý ÁõÈıº
  • dysuria-pyuria syndrome
    ¹è´¢ Àå¾Ö-³ó´¢ ÁõÈıº
  • early postprandial postgastrectomy syndrome
    Á¶±â ½ÄÈļº À§ ÀýÁ¦ ÈÄ ÁõÈıº
  • eaton-lambert syndrome
    ÀÌÆ°-¶÷¹öÆ® ÁõÈıº
  • ectopic ACTH syndrome
    À̼Ҽº ºÎ½Å ÇÇÁú ÀÚ±Ø È£¸£¸ó ÁõÈıº, À̼Ҽº ACTH ÁõÈıº
    ACTHÀÇ °úÀ× »ý»ê, Á߽ɼº ºñ¸¸, ¸¸¿ùÇü ¾ó±¼, °íÇ÷¾Ð µîÀÇ Áõ»óÀÌ ³ªÅ¸³­´Ù.
  • ectopic Cushing's syndrome
    À̼Ҽº Äí½Ì ÁõÈıº
  • Edinger-Westphal syndrome
    ¿¡µù°Å-¿þ½ºÆ®ÆÈ ÁõÈıº
  • effort syndrome
    ¿¡Æ÷Æ® ÁõÈıº
  • electrolyte deficiency syndrome
    ÀüÇØÁú °áÇÌ ÁõÈıº
  • empty sella syndrome
    °ø Å;îŰ¾È ÁõÈıº
    °¡Àå ÈçÇϰԴ ÁöÁÖ¸·ÀÌ Å;îŰ¾È Ⱦ°Ý¸·ÀÇ °á¼ÕºÎ¸¦ ÅëÇÏ¿© ºüÁ® µé¾î¿À´Â °ÍÀε¥ Çϼöü °æÀÌ Áö³ª´Â ±¸¸ÛÀÌ Å©´ÙµçÁö ¶Ç´Â ´Ù¸¥ °á¼ÕºÎ°¡ ÀÖ¾î ÀϾ´Ù. ³ú ô¼ö¾×¾ÐÀ¸·Î ÀÎÇØ Çϼöü°¡ À§ÃàµÇ°í Å;îŰ¾ÈÀº ºó ¸ð½ÀÀÌ µÈ´Ù. ´Ù¸¥ ¿øÀÎÀ¸·Î´Â Sheehan ÁõÈıº, ¼±Á¾ÀÇ ¿ÏÀü °æ»ö ÈÄ ¼¶À¯¼º ¹ÝÈçÈ­ ±×¸®°í ¼ö¼úÀ̳ª ¹æ»ç¼±Àû Çϼöü ÀýÁ¦ µîÀÌ´Ù. ´ë°³ ȯÀÚ´Â Çϼöü ºÎÀüÀ» ¹æÁöÇÒ ¸¸ÇÑ ÃæºÐÇÑ ½ÇÁúÀÌ º¸Á¸µÈ´Ù. ±×·¯³ª ¶§·Î´Â Ç⼺ È£¸£¸ó ÇÑ Á¾·ù ¶Ç´Â ±× ÀÌ»óÀÇ ºÐºñ ºÎÁ·ÀÌ ÀÖ´Ù.
  • encephalitis syndrome
    ³ú¿° ÁõÈıº
  • encephalotrigeminal syndrome
    ³ú »ïÂ÷ ½Å°æ ÁõÈıº
  • eosinophilia myalgia syndrome
    È£»ê±¸¼º ±ÙÀ°Åë ÁõÈıº, È£»ê±¸ Áõ´Ù¼º ±ÙÀ°Åë ÁõÈıº
  • eosinophilic pulmonary syndrome
    È£»ê¼º Æó ÁõÈıº
    ¸¸¼º È£»ê±¸¼º Æó·ÅÀº ÆóÆ÷ ¼¼Ã´À̳ª »ý°Ë»ó È£»ê±¸°¡ Æó Á¶Á÷ÀÇ ¸»Ãʺο¡ Ä§ÂøµÈ ¼Ò°ßÀ» Ư¡À¸·Î ÇÏ´Â ÁõÈıºÀ» ÀǹÌÇÑ´Ù. Ç÷¾× È£»ê±¸ Áõ°¡°¡ ´ëºÎºÐ °üÂûµÈ´Ù. ¸¸¼º È£»ê±¸¼º Æó·ÅÀº ÁÖ·Î ¿©ÀÚ¿¡ ³ªÅ¸³ª¸ç, ¹ß¿­, ¹ßÇÑ, üÁß °¨¼Ò, È£Èí °ï¶õÀÌ Æ¯Â¡ÀÌ´Ù. Ä¡·á´Â °æ±¸
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adiposogenital syndrome A disorder characterised primarily by obesity and hypogonadotrophic hypogonadism in adolescent boys; dwarfism is rare, and when present is thought to reflect hypothyroidism. Visual loss, behavioural abnormalities, and diabetes insipidus may occur. Frohlich's syndrome often is used synonymously for this disorder, although the original case involved a pituitary tumour; most cases are thought to result from hypothalamic dysfunction in areas regulating appetite and gonadal development. The most common causes are pituitary and hypothalamic neoplasms.
Synonym: adiposis orchica, adiposogenital degeneration, adiposogenital dystrophy, adiposogenital syndrome, hypophysial syndrome, hypothalamic obesity with hypogonadism.
Origin: L. Fr. G. Dys-, bad, + trophe, nourishment
(05 Mar 2000)
adrenal cortical syndrome <syndrome> An inexact (and obsolete) term that has been applied to Cushing's syndrome, Addison's disease, or the adrenogenital syndrome.
(05 Mar 2000)
adrenal virilizing syndrome Virilism produced by excessive or abnormal secretory patterns of adrenocortical steroids.
Synonym: adrenal virilizing syndrome.
(05 Mar 2000)
adrenogenital syndrome <syndrome> A general term for a group of disorders which involve hyperplasia (or malignant tumours) of the adrenal cortex. Features include masculinisation of women, feminisation of men or precocious sexual development of children.
(27 Sep 1997)
adult respiratory distress syndrome <chest medicine, syndrome> A clinical syndrome that includes pulmonary insufficiency. It is a descriptive term that is applied to a variety of diffuse infiltrative processes in the lung.
Manifestations include severe shortness of breath, rapid breathing and arterial hypoxaemia (low oxygen). Chest X-ray shows bilateral diffuse infiltrates.
Treatment most often includes mechanical respiratory support. Causes include toxic gas (chlorine, NO2, smoke) exposure, severe metabolic derangement, gastric acid aspiration, pancreatitis, sepsis and trauma.
Acronym: ARDS
(12 Jul 2000)
afferent loop syndrome <syndrome> A complication of gastrojejunostomy, caused by acute or chronic obstruction of the afferent loop due to hernia, intussusception, kinking, volvulus, etc. It is characterised by pain and vomiting of bile-stained fluid and includes acute afferent loop obstruction and bilious vomiting.
(12 Dec 1998)
aglossia-adactylia syndrome <syndrome> Congenital absence or hypoplasia of the tongue, associated with absence of the digits.
(05 Mar 2000)
Ahumada-Del Castillo syndrome <syndrome> Unphysiological lactation and amenorrhoea not following pregnancy characterised by hyperprolactinaemia and a pituitary adenoma.
Synonym: Argonz-Del Castillo syndrome.
(05 Mar 2000)
Aicardi's syndrome <syndrome> Agenesis of the corpus collosum with infantile spasms in female babies.
(05 Mar 2000)
alagille syndrome <syndrome> Hypoplasia of the hepatic ducts, congenital pulmonary artery stenosis, facial abnormalities, and other congenital malformations, particularly skeletal. It is often presented as jaundice during the neonatal period. It is an autosomal recessive disease generally manifesting during childhood. "arteriohepatic" refers to the pulmonary artery and the intrahepatic bile ducts, not to the hepatic artery.
(12 Dec 1998)
Albright's syndrome <syndrome> A condition of cystic bone growth that results from abnormal bone development. May occur with bone lesions, skin pigmentation and endocrine abnormalities.
See: McCune-Albright syndrome.
(27 Sep 1997)
alcohol amnestic syndrome <syndrome> An amnestic syndrome resulting from alcoholism; alcoholic "blackouts." Cf.: Korsakoff's syndrome.
(05 Mar 2000)
Aldrich syndrome <syndrome> An sex-linked (X chromosome) genetic disorder occurring in male children that is characterised by thrombocytopenia, eczema, melena and susceptibility to bacterial infections. Death often occurs from severe haemorrhage or overwhelming sepsis.
Inheritance: sex-linked (X chromosome).
(27 Sep 1997)
Alezzandrini's syndrome <syndrome> A rare syndrome appearing in adolescents and young adults, characterised by unilateral degenerative retinitis, followed by ipsilateral poliosis and facial vitiligo, and occasionally bilateral perceptive deafness.
(05 Mar 2000)
Alice in Wonderland syndrome <syndrome> The illusion of dreams, feelings of levitation, and alteration in the sense of the passage of time, sometimes associated with migraine, epilepsy, and various diseases of the parietal lobe of the brain.
(05 Mar 2000)
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